Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

M. Vermaat · SciRah

Researcher profile · Semantic Scholar

M. Vermaat

Share profile

M. Vermaat — researcher profile on SciRah

h-index: 22
Works: 36
Citations: 2,820

Most-cited papers

Disease variants alter transcription factor levels and methylation of their binding sites
M. Bonder, R. Luijk, D. Zhernakova, Matthijs Moed +51 more
2016Nature Genetics433 citations Open access
Semantic Scholar
Identification of context-dependent expression quantitative trait loci in whole blood
D. Zhernakova, Patrick Deelen, M. Vermaat, M. van Iterson +43 more
2016Nature Genetics420 citations Open access
Semantic Scholar
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C Androniki Sara L Freerk Pier Francesco Clara C P Francioli Menelaou Pulit van Dijk Palamara Elbers, L. Francioli, A. Menelaou, S. Pulit +82 more
2014Nature Genetics308 citations Open access
Semantic Scholar
The Genome of the Netherlands: design, and project goals
D. Boomsma, C. Wijmenga, E. Slagboom, M. Swertz +48 more
2013European Journal of Human Genetics289 citations Open access
Semantic Scholar
A linear mixed model approach to study multivariate gene-environment interactions
R. Moore, F. Casale, M. Bonder, D. Horta +51 more
2018Nature Genetics156 citations Open access
Semantic Scholar
Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations
Sonia H. Shah, M. Bonder, R. Marioni, Zhihong Zhu +67 more
2015American Journal of Human Genetics142 citations Open access
Semantic Scholar
Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour
M. Mills, Felix C. Tropf, D. Brazel, N. V. van Zuydam +202 more
2021Nature Human Behaviour130 citations Open access
Semantic Scholar
Full-length mRNA sequencing uncovers a widespread coupling between transcription initiation and mRNA processing
S. Anvar, Guy Allard, Elizabeth Tseng, Gloria M. Sheynkman +8 more
2018Genome Biology124 citations Open access
Semantic Scholar
Mutalyzer 2: next generation HGVS nomenclature checker
Mihai Lefter, J. Vis, M. Vermaat, J. D. den Dunnen +2 more
2020bioRxiv98 citations Open access
Semantic Scholar
Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck
MingKun Li, R. Rothwell, M. Vermaat, Manja Wachsmuth +15 more
2016Genome Research84 citations Open access
Semantic Scholar
Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects
T. Vrijenhoek, K. Kraaijeveld, M. Elferink, J. de Ligt +44 more
2015European Journal of Human Genetics75 citations Open access
Semantic Scholar
Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs
I. Ricaño-Ponce, D. Zhernakova, Patrick Deelen, O. Luo +62 more
2016Journal of Autoimmunity74 citations Open access
Semantic Scholar
A SNP panel for identification of DNA and RNA specimens
S. Yousefi, Tooba Abbassi-Daloii, T. Kraaijenbrink, M. Vermaat +60 more
2018BMC Genomics50 citations Open access
Semantic Scholar
Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly
Artem Kim, Clara Savary, C. Dubourg, W. Carré +100 more
2018Brain : a journal of neurology49 citations Open access
Semantic Scholar
Comprehensive evaluation of smoking exposures and their interactions on DNA methylation
Thanh T. Hoang, Yun-Sung Lee, D. McCartney, E. Kersten +71 more
2024EBioMedicine43 citations Open access
Semantic Scholar
Epigenome-wide association study of ADHD symptoms in adults
J. van Dongen, Nuno R Zilhao, K. Sugden, E. Hannon +58 more
2019Biological Psychiatry36 citations Open access
Semantic Scholar
Determining the quality and complexity of next-generation sequencing data without a reference genome
S. Anvar, L. Khachatryan, M. Vermaat, M. V. van Galen +7 more
2014Genome Biology32 citations Open access
Semantic Scholar
An efficient algorithm for the extraction of HGVS variant descriptions from sequences
J. Vis, M. Vermaat, P. Taschner, Joost N. Kok +1 more
2015Bioinform.30 citations Open access
Semantic Scholar
Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects
T. Vrijenhoek, K. Kraaijeveld, M. Elferink, J. de Ligt +44 more
2015European Journal of Human Genetics26 citations Open access
Semantic Scholar
Autosomal genetic variation is associated with DNA methylation in regions variably escaping X-chromosome inactivation
R. Luijk, Hao-Yu Wu, Cavin K. Ward-Caviness, E. Hannon +58 more
2018Nature Communications25 citations Open access
Semantic Scholar
Genome-wide identification of directed gene networks using large-scale population genomics data
R. Luijk, K. Dekkers, M. van Iterson, Wibowo Arindrarto +49 more
2017Nature Communications24 citations Open access
Semantic Scholar
Disease variants alter transcription factor levels and methylation of their binding sites
M. Bonder, R. Luijk, D. Zhernakova, Matthijs Moed +51 more
2015bioRxiv21 citations Open access
Semantic Scholar
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies.
Anke R. Hammerschlag, E. Byrne, M. Bartels, N. Wray +118 more
2020Biological Psychiatry19 citations Open access
Semantic Scholar
Whole genome sequencing and the application of a SNP panel reveal primary evolutionary lineages and genomic variation in the lion (Panthera leo)
L. Bertola, M. Vermaat, F. Lesilau, M. Chege +9 more
2019bioRxiv18 citations Open access
Semantic Scholar
Hypothesis-free identification of modulators of genetic risk factors
D. Zhernakova, Patrick Deelen, M. Vermaat, M. van Iterson +42 more
2015bioRxiv18 citations Open access
Semantic Scholar
Integrated Whole Genome and Transcriptome Analysis Identified a Therapeutic Minor Histocompatibility Antigen in a Splice Variant of ITGB2
M. Pont, Dyantha I. van der Lee, E. D. van der Meijden, C. V. van Bergen +9 more
2016Clinical Cancer Research16 citations
Semantic Scholar
DNA methylation in peripheral tissues and left-handedness
V. Odintsova, M. Suderman, F. Hagenbeek, D. Caramaschi +63 more
2021Scientific Reports15 citations Open access
Semantic Scholar
WGS-based telomere length analysis in Dutch family trios implicates stronger maternal inheritance and a role for RRM1 gene
Lilit Nersisyan, M. Nikoghosyan, A. Arakelyan, L. Francioli +83 more
2019Scientific Reports10 citations Open access
Semantic Scholar
Full-length mRNA sequencing uncovers a widespread coupling between transcription and mRNA processing
S. Anvar, Guy Allard, Elizabeth Tseng, Gloria M. Sheynkman +8 more
2017bioRxiv5 citations Open access
Semantic Scholar
The Genome of the Netherlands design, and project goals
D. Boomsma, C. Wijmenga, E. Slagboom, M. Swertz +48 more
4 citations
Semantic Scholar
Whole genome sequencing and the application of a SNP panel reveal primary evolutionary lineages and genomic variation in the lion (Panthera leo)
L. D. Bertola, M. Vermaat, F. Lesilau, M. Chege +9 more
2022BMC Genomics0 citations Open access
Semantic Scholar
Publisher Correction: Identification of 371 genetic variants for age at first sex and birth linked to externalising behavior
M. Mills, Felix C. Tropf, D. Brazel, N. V. van Zuydam +202 more
2021Nature Human Behaviour0 citations Open access
Semantic Scholar
University of Groningen Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families
MingKun Li, R. Rothwell, M. Vermaat, Manja Wachsmuth +15 more
20160 citations
Semantic Scholar
Chapter 4 Aging is associated with increased incidence of alternative splicing
I. Pulyakhina, V. Takhaveev, M. Vermaat, M. van Iterson +2 more
20160 citations
Semantic Scholar
Integrated whole genome and transcriptome analysis identified a therapeutic minor histocompatibility antigen encoded by an alternative ITGB2 transcript
M. Pont, Dyantha I. van der Lee, E. D. van der Meijden, C. V. van Bergen +9 more
2015Journal of Immunotherapy for Cancer0 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

P. 't Hoen×22
Invite
P. 't Hoen — researcher profile on SciRah
F. van Dijk×21
Invite
F. van Dijk — researcher profile on SciRah
M. Beekman×21
Invite
M. Beekman — researcher profile on SciRah
M. Swertz×20
Invite
M. Swertz — researcher profile on SciRah

×19

Invite

J. Hottenga — researcher profile on SciRah

C. Wijmenga×18

Invite

C. Wijmenga — researcher profile on SciRah

Invite

J. Veldink — researcher profile on SciRah

C. M. van Duijn×18

Invite

C. M. van Duijn — researcher profile on SciRah

M. van Iterson×17

Invite

M. van Iterson — researcher profile on SciRah

M. V. van Galen×17

Invite

M. V. van Galen — researcher profile on SciRah

Invite

J. Bot — researcher profile on SciRah

Invite

L. Franke — researcher profile on SciRah